Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology

  • University of Washington Center for Mendelian Genomics

Research output: Contribution to journalComment/debatepeer-review

1 Scopus citations

Abstract

[This corrects the article DOI: 10.1016/j.xhgg.2022.100102.].

Original languageEnglish (US)
Pages (from-to)100168
Number of pages1
JournalHuman Genetics and Genomics Advances
Volume4
Issue number1
DOIs
StatePublished - Jan 12 2023

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics(clinical)

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